Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00941278 · ClinicalTrials.gov registry record · Phase 2

An Efficacy and Safety Study of PH-10 Aqueous Hydrogel for the Treatment of Plaque Psoriasis

A Phase 2 study, sponsored by Provectus Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
30
Enrollment target

NCT00941278: Completed Phase 2 study, sponsored by Provectus Pharmaceuticals.

NCT00941278 is a Phase 2 study that has completed, run by Provectus Pharmaceuticals. The registered enrollment target is 30 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00941278, a Phase 2 study, has completed, sponsored by Provectus Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
30 participants
Enrollment target

Study Summary

PH-10 is an aqueous hydrogel formulation of rose bengal disodium (RB) for topical administration to the skin, and is being studied for the treatment of cutaneous skin disorders, specifically psoriasis and atopic dermatitis. This phase 2 efficacy and safety study will assess topical PH-10 applied once daily to areas of mild to moderate plaque psoriasis.

Interventions

  • DRUG PH-10 (0.001% Rose Bengal)

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2009-07
Est. Completion 2010-04
Phase Phase 2
Provectus Pharmaceuticals

6 total trials

What the finished NCT00941278 record still lists

NCT00941278 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 1 intervention - of which PH-10 (0.001% Rose Bengal) is the first listed.

NCT00941278 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00941278 about?

NCT00941278 is a clinical study titled "An Efficacy and Safety Study of PH-10 Aqueous Hydrogel for the Treatment of Plaque Psoriasis". PH-10 is an aqueous hydrogel formulation of rose bengal disodium (RB) for topical administration to the skin, and is being studied for the treatment of cutaneous skin disorders, specifically psoriasis and atopic dermatitis. This phase 2 efficacy and safety study will assess topical PH-10 applied onc...

What is the current status of trial NCT00941278?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2009-07. Estimated completion is 2010-04.

What interventions are being tested in trial NCT00941278?

The interventions under investigation include: PH-10 (0.001% Rose Bengal) (DRUG).

Who is sponsoring clinical trial NCT00941278?

This trial is sponsored by Provectus Pharmaceuticals, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00941278's enrollment target sits among peer trials

30 1582nd of 2000 higher than 332 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00977977 · 30 participants · Phase 2

    Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy

  • NCT01459107 · 30 participants · Phase 2

    Human Upper Extremity Allotransplantation

  • NCT01666080 · 30 participants · NA

    Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)

  • NCT01720836 · 30 participants · Phase 1

    Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00941278, the US trial registry maintained by the National Library of Medicine. NCT00941278 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.